Journal of biochemical and molecular toxicology · 2003
Ultraviolet radiation modulates nuclear factor kappa B activation in human lens epithelial cells.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Boileau Thomas W-M, Bray Tammy M, Bomser Joshua A
Аннотация
Exposure to ultraviolet radiation (UVR) is a known risk factor for cataract, but the molecular mechanisms involved have not been elucidated. We hypothesized that exposure to UVR would modulate the activation of nuclear factor kappa-B (NF-kappa B) within the human lens epithelium, since NF-kappa B is a key regulator of cellular responses to UVR stress in other cell types. Human lens epithelial (HLE) cells were exposed to acute physiological doses of ultraviolet A (UVAR), B (UVBR), C (UVCR) radiation, or interleukin-1 beta (IL-1 beta) and NF-kappa B activation was measured by electrophoretic shift assay (EMSA). Phosphorylation of I kappa B in response to UVAR was measured by Western blotting. Irradiation of HLE cells with UVAR (0-1100 J/m(2)) did not reduce cell survival, while UVBR (400-1600 J/m(2)) and UVCR (300-900 J/m(2)) significantly reduced HLE cell survival. EMSA analysis of HLE nuclear proteins indicated activation of NF-kappa B, but not activator protein-1 (AP-1), by UVAR. The effects of UVBR and UVCR were less pronounced. Exposure of HLE cells to UVAR (0-900 J/m(2)) followed by a 30-min incubation resulted in a dose-dependent activation of NF-kappa B. UVAR-induced NF-kappa B activation in HLE cells was evident 10 min postirradiation, maximal at 60 min and returned to control levels by 120 min. Western blot analysis of phosphorylation of the NF-kappa B inhibitory protein, I kappa B, revealed that UVAR activates NF-kappa B via a mechanism involving the phosphorylation of I kappa B-alpha; this effect was dose-dependent. Supershift analysis demonstrated that UVAR and IL-1 beta activate the transcriptionally active p65/p50 NF-kappa B dimer. These studies demonstrate that UVAR activates NF-kappa B in HLE cells in a time- and dose-dependent manner via signaling through I kappa B-alpha. The activation of NF-kappa B in HLE cells by UVAR may have implications for the development and progression of cataract and other related ocular disorders.